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Pompe disease (glycogen storage disease type II) : clinical features and enzyme replacement therapyVAN DER BEEK, N. A. M. E; HAGEMANS, M. L. C; VAN DER PLOEG, A. T et al.Acta neurologica belgica. 2006, Vol 106, Num 2, pp 82-86, issn 0300-9009, 5 p.Article

Visual Hallucinations in a Patient with Adult Onset Acid Maltase Deficiency DisorderPATIL, Ritesh; DEPRIEST, Jack L.Journal of general internal medicine. 2009, Vol 24, Num 5, pp 683-686, issn 0884-8734, 4 p.Article

Pompe disease in a Brazilian series: clinical and molecular analyses with identification of nine new mutationsOBA-SHINJO, Sueli M; DA SILVA, Roseli; MUNOZ, Verônica et al.Journal of neurology. 2009, Vol 256, Num 11, pp 1881-1890, issn 0340-5354, 10 p.Article

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BOTH TYPE 1 AND TYPE 2a MUSCLE FIBERS CAN RESPOND TO ENZYME THERAPY IN POMPE DISEASEDROST, Maarten R; SCHAART, Gert; VAN DIJK, Paul et al.Muscle & nerve. 2008, Vol 37, Num 2, pp 251-255, issn 0148-639X, 5 p.Article

Morphological changes in muscle tissue of patients with infantile Pompe's disease receiving enzyme replacement therapyWINKEL, Léon P. F; KAMPHOVEN, Joep H. J; VAN DEN HOUT, Hannerieke J. M. P et al.Muscle & nerve. 2003, Vol 27, Num 6, pp 743-751, issn 0148-639X, 9 p.Article

DIAGNOSTIC CRITERIA FOR LATE-ONSET (CHILDHOOD AND ADULT) POMPE DISEASEMuscle & nerve. 2009, Vol 40, Num 1, pp 149-160, issn 0148-639X, 12 p.Article